Author

Chuanchun Yang

Observed name: Chuan‐Chun Yang

Observed institutions: BGI Group (China), Guangdong Medical College, Hunan Children's Hospital, University of South China

ORCID: 0000-0002-7478-3218

Observed ORCID: 0000-0002-7478-3218

OpenAlex ID: A5046488296

A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole-Genome Low-Coverage Sequencing

2014 · Zirui Dong, Lupin Jiang, et al. · Human Mutation · 105

Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocation

2014 · Yongjia Yang, Chuanchun Yang, et al. · Genomics · 48

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Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic male

2014 · Lin Li, Haixiao Chen, et al. · Gene · 19

Successful pregnancy after prenatal diagnosis by NGS for a carrier of complex chromosome rearrangements

2020 · Jian Ou, Chuanchun Yang, et al. · Reproductive Biology and Endocrinology · 16

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Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report study

2016 · Hui Yao, Chuanchun Yang, et al. · BMC Medical Genetics · 15

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Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings

2018 · Aixiang Luo, Dehua Cheng, et al. · Molecular Cytogenetics · 12

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Complete genome sequencing and variant analysis of a Pakistani individual

2013 · Muhammad Kamran Azim, Chuanchun Yang, et al. · Journal of Human Genetics · 12

Systematic analysis of microbiota in pregnant Chinese women and its association with miscarriage

2022 · Yu Guang, Xiao Shen, et al. · Annals of Translational Medicine · 10

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Successful birth after preimplantation genetic testing for a couple with two different reciprocal translocations and review of the literature

2021 · Dun Liu, Chuangqi Chen, et al. · Reproductive Biology and Endocrinology · 8

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Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissue

2019 · Qian Geng, Xiaoli Cui, et al. · Journal of Assisted Reproduction and Genetics · 8

Analysis of complex chromosomal rearrangements using a combination of current molecular cytogenetic techniques

2022 · Ping He, Xiaoni Wei, et al. · Molecular Cytogenetics · 7

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A case report of congenital idiopathic hypogonadotropic hypogonadism caused by novel mutation of GNRHR gene

2021 · Liping Wang, Weisheng Lin, et al. · Medicine · 5

Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques

2016 · Qiong Pan, Hao Hu, et al. · PLoS ONE · 4

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Highly precise breakpoint detection of chromosome balanced translocation in chronic myelogenous leukaemia: Case series

2022 · Chuanchun Yang, Xiaoli Cui, et al. · Journal of Cellular and Molecular Medicine · 3

Identification and interruption of inheritance of familial cryptic translocations: A case report

2024 · Jian Ou, Jian Sun, et al. · Molecular Genetics & Genomic Medicine · 2

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Highly precise breakpoint detection of chromosome balanced translocation in a Chronic Myelogenous Leukemia patient

2021 · Chuanchun Yang, Xiaoli Cui, et al. · Research Square

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A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report

2021 · Dalin Fu, Weisheng Lin, et al. · BMC Pediatrics

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Breakpoints Identification of a Balanced Complex Chromosome Rearrangement Case: 46,XX, t(6;15;10;9)(q13;q15;p11.2;q34.3) ins(9;8)(q22.33;q21.1q21.3)

2021 · Bohong Li, Suli Li, et al. · Clinical Laboratory

The Novel Mutations of Unexplained Abortion Were Analyzed at the Nucleotide Level and Classified According to Gene Function

2020 · Ji Yao, Peishan Chen, et al. · Research Square

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Works count: 19

Citation count: 274

H-index: 8

I10-index: 8